Photodissociation of CO2 via the 1Πg state: Wavelength-dependent imaging studies of O(1D2) photoproducts.

Abstract

Photodissociation of CO2 via the 1Πg state is investigated using a time-sliced velocity-mapped ion imaging apparatus combined with a tunable vacuum ultraviolet photolysis source. The main O(1D2) + CO(X1Σ+) channel is directly observed from the measured images of O(1D2) photoproducts at 129.08-134.76nm. The total kinetic energy release spectra determined based on these images show that the energetic thresholds for the O(1D2) + CO(X1Σ+) photoproducts correspond to the thermochemical thresholds for the photodissociation of CO2(v2 = 0) and CO2(v2 = 1). One significant difference among the CO(X1Σ+, v) vibrational distributions for the predominant CO2(v2 = 0) dissociation is that the population of CO(v = 0) becomes favorable at 130.23-133.45nm compared to the Boltzmann-like component (v > 0) that always exists at 129.08-134.76nm. The wavelength dependences of the overall β are found to follow the variation trend of the CO(v = 0) abnormal intensity. The vibrational state-specific β values present a roughly decreasing trend with an increase in v, whereas β(v = 0) appears to be significantly larger than β(v = 1) at 130.23-133.45nm compared to 134.76 and 129.08nm. The non-statistical CO(v = 0) with larger β values at 130.23-133.45nm implies that an additional pathway may open through the conical intersection coupling to the dissociative 21A'  state, except for the ever-existing pathway that yields the Boltzmann-like component. In contrast, at 129.08nm, the restoration of the statistical equilibrium in the CO(X1Σ+, v) vibrational distribution may be caused by the emergence of novel dissociation pathways arising from the participation of the 31A″ state.